30168-33-3

Basic information

• Product Name: Ethanone,2-[(4-chlorophenyl)thio]-1-phenyl-
• Synonyms: Acetophenone,2-[(p-chlorophenyl)thio]- (6CI,7CI,8CI); NSC 35979; p-Chlorophenyl phenacylsulfide; a-(p-Chlorophenylthio)acetophenone
• CAS NO: 30168-33-3
• Molecular Formula: C₁₄H₁₁ClOS
• Molecular Weight: 262.7545
• Mol File: 30168-33-3.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 396.7°Cat760mmHg
• Flash Point: 193.7°C
• Density: 1.27g/cm³
• CAS DataBase Reference: Ethanone,2-[(4-chlorophenyl)thio]-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone,2-[(4-chlorophenyl)thio]-1-phenyl-(30168-33-3)
• EPA Substance Registry System: Ethanone,2-[(4-chlorophenyl)thio]-1-phenyl-(30168-33-3)

Safety Data

• Hazardous Substances Data: 30168-33-3(Hazardous Substances Data)

Upstream product

• 532-27-4 1-chloroacetophenone 
• 18803-44-6 sodium p-chlorothiophenolate 
• 70-11-1 α-bromoacetophenone 
• 3226-37-7 4-chlorophenyl thiocyanate 
• 5633-34-1 (benzoylmethylene)dimethylsulfurane 
• 30718-19-5 (4-chlorophenylthio)trimethylsilane 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 106-54-7 p-Chlorothiophenol 
• 933-01-7 4-chloro-benzenesulfenyl chloride 
• 120-46-7 1,3-diphenylpropanedione 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 98-88-4 benzoyl chloride 
• 1021-45-0 phosphoric acid diethyl ester-(1-phenyl-vinyl ester) 
• 98-86-2 acetophenone 

Downstream Products

• 19968-36-6 5-(4-chloro-phenylsulfanyl)-4-phenyl-3H-thiazol-2-one 
• 17530-91-5 2-((4-chlorophenyl)sulfinyl)-1-phenylethan-1-one 
• 54720-50-2 2-bromo-2-(4-chloro-phenylsulfanyl)-1-phenyl-ethanone 
• 338794-35-7 2-(4-Chloro-phenylsulfanyl)-1-phenyl-ethanone oxime 
• 187672-55-5 [4-(4-Chloro-phenylsulfanyl)-3-phenyl-isoxazol-5-yl]-acetic acid methyl ester 
• 153235-46-2 7-(4-Chloro-phenylsulfanyl)-3-methyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 153235-47-3 7-(4-Chloro-phenylsulfanyl)-3-ethyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 153235-48-4 7-(4-Chloro-phenylsulfanyl)-3,6-diphenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 153235-49-5 7-(4-Chloro-phenylsulfanyl)-6-phenyl-3-p-tolyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 106-54-7 p-Chlorothiophenol 
• 1180676-96-3 ethyl (E)-4-(4-chlorophenoxy)-3-phenylbut-2-enoate 
• 1235497-54-7 4-(4-chlorophenyl)-5-[(4-chlorophenyl)sulfanyl]-2-methoxy-6-phenylnicotinonitrile 
• 1260255-00-2 2-[(4-chlorophenyl)sulfanyl]-1-phenyl-1-ethanone N-(Z)-2-[(4-chlorophenyl)sulfanyl]-1-phenylethylidenehydrazone 
• 1380501-91-6 methyl(4-chlorophenyl)sulfonium phenacylide 

Relevant articles and documents

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Iridium-Catalyzed Carbenoid Insertion of Sulfoxonium Ylides for Synthesis of Quinoxalines and β-Keto Thioethers in Water

Sulfoxonium ylides as safe carbene precursors are described for iridium-catalyzed carbene insertions and annulation, providing a facile and green approach to access a variety of quinoxaline derivatives in water. This water-mediated method also allows the preparation of β-keto thioethers under mild condition.

KI/K 2 S 2 O 8 -Mediated α-C-H Sulfenylation of Carbonyl Compounds with (Hetero)Aryl Thiols

A new and facile KI/K 2 S 2 O 8 -mediated α-C-H sulfenylation of carbonyl compounds with (hetero)aryl thiols was developed for the formation of C-S bond at room temperature. This method provided a simple process for the sy